Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Aplasia of the fingers (HP:0009380)

Grandparent Node:
Oligodactyly (HP:0012165)

Parent Node:
Hand oligodactyly (HP:0001180)

..Starting node
..Postaxial oligodactyly (HP:0006210)

Term ID:

6210

Name:

Postaxial oligodactyly

Synonym:

Definition:

Comments:

Reference:

HP:0006210

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hand monodactyly (HP:0004058)

Unilateral oligodactyly (HP:0006230)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006210	HP:0006210	Postaxial oligodactyly	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.